PEMF therapy devices have been used in clinical settings for decades, with origins in orthopedic bone healing research from the 1970s. FDA-cleared and clinically established. Luci Medical provides the devices, clinical education, and support to add it to your practice.
How We Work
PEMF stands for pulsed electromagnetic field therapy. The device delivers controlled, low-frequency electromagnetic waves to targeted areas of the body. Published research has documented PEMF's role in modulating inflammatory processes at the cellular level.[1] These waves pass through the skin to the treatment area within the parameters established by the device's FDA clearance.
PEMF therapy devices are FDA-cleared Class II medical devices. The primary cleared indication is for the adjunctive treatment of non-union fractures. The technology has been used in clinical settings for decades, with roots in orthopedic bone healing research dating back to the 1970s.
Sessions are administered with the patient fully clothed. No needles, no incisions, no recovery time. The device does the work while your patient sits comfortably.
Applications
PEMF has its deepest clinical history in bone healing applications. A meta-analysis of 22 RCTs (1,468 participants) found PEMF increased bone healing rates compared to controls.[2] A separate systematic review of 17 RCTs (1,197 patients) examined PEMF for osteoarthritis.[3] The FDA clearance for non-union fractures makes this a natural fit for orthopedic and sports medicine practices.
PEMF devices are within scope for chiropractic practices in Florida. For DCs looking to expand beyond manual therapies, this is one of the few FDA-cleared device categories available. Rehabilitation practices can incorporate sessions into existing patient workflows with minimal disruption.
If your practice focuses on patient wellness and recovery, PEMF therapy devices may fit as a complementary offering. A multi-center RCT of 120 patients across 5 orthopedic centers found PEMF achieved a 36% pain reduction compared to 10% for standard care.[4] The treatment requires no needles or incisions, and the short session times make it straightforward to incorporate alongside your current services.
Service Integration
PEMF therapy fits naturally alongside other device services, especially in practices focused on musculoskeletal care and patient recovery.
Shockwave therapy is the most common pairing. Both serve orthopedic and sports medicine patients, and the combination gives your practice two distinct, billable treatment modalities for overlapping patient populations. Learn more.
Red light therapy adds a near-zero consumable cost complement for practices that want a broader device menu. Its short sessions and simple operation make it easy to incorporate without disrupting existing workflows. Learn more.
Luci Medical supports multi-device practices with consolidated ordering, combined clinical education, and a single point of contact for your device portfolio.
For Providers
PEMF therapy is a cash-pay service line with low per-session consumable costs. Most systems require no disposables.
Not all PEMF devices are the same. The category spans a wide range of form factors, intensity levels, and price points. Choosing the right device depends on your practice type, patient volume, and clinical applications.
Luci Medical helps you select the right device category for your practice model. We evaluate your patient mix, treatment room setup, and volume expectations before recommending a system.
| Category | Form Factor | Typical Use | Investment Range |
|---|---|---|---|
| Low-intensity portable | Handheld or small mat | Individual treatment areas, patient home use programs | Lower entry point |
| Mid-to-high clinical | Clinical-grade applicators, higher output | In-office treatment sessions, dedicated treatment rooms | Mid-range investment |
| Mat-style systems | Full-body treatment mats | Whole-body sessions, wellness and recovery protocols | Varies by system |
PEMF therapy uses gentle electromagnetic pulses delivered through a device placed near or on the treatment area. You stay fully clothed during the session. There are no needles and nothing invasive about the process.
What a typical visit looks like:
PEMF is generally delivered as a series of sessions rather than a one-time treatment. Your provider will evaluate whether it is appropriate for your specific situation and create a plan based on your needs and health history.
Important safety information: PEMF therapy is not appropriate for everyone. Your provider will screen for contraindications, which include metallic implants in the treatment area, cardiac pacemakers or other implanted electronic devices, and pregnancy. Always discuss your full medical history with your provider before starting any new treatment.
Training
Getting a device into your practice is step one. Running it effectively and responsibly is where Luci Medical adds the most value.
Your team handles the clinical work. We handle device selection, education, contraindication guidance, and ongoing technical support.
Device operation training for your clinical team, covering settings, positioning, and session management.
We help you develop your own protocols based on current industry guidelines and your clinical workflow.
Contraindication screening procedures and documentation templates for metallic implants, pacemakers, and pregnancy.
Technical support and clinical consultation as your PEMF program grows.
Common Questions
Important Disclosures
Device disclaimer
PEMF therapy devices distributed by Luci Medical are FDA-cleared Class II medical devices. The primary cleared indication is for the adjunctive treatment of non-union fractures. Clinical applications are determined by the treating provider's clinical judgment. Uses beyond the device's cleared indication are not cleared by FDA. Clinical application decisions rest with the treating provider. Luci Medical provides published clinical literature to support informed decision-making.
Clinical outcomes
Individual clinical outcomes vary based on patient health, condition, and clinical protocol. Clinical applications of PEMF beyond the device's cleared indication have not been evaluated or cleared by FDA.
Financial disclaimer
Revenue and financial estimates represent general market observations. Actual practice revenue depends on patient volume, pricing, market conditions, and operational factors. These are not projections of your practice performance.
A 15-minute call to discuss devices, economics, and implementation for your practice.
